Variant #0000510856 (NC_000002.11:g.179414964T>A, NM_001267550.1:c.91601A>T (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.179414964T>A
DNA change (hg38) g.178550237T>A
Published as TTN(NM_001256850.1):c.86678A>T (p.(Asp28893Val)), TTN(NM_001267550.1):c.91601A>T (p.D30534V), TTN(NM_001267550.2):c.91601A>T (p.D30534V), TTN(NM_1...)
ISCN -
DB-ID TTN_000874 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00082 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 -?/. - c.91601A>T r.(?) p.(Asp30534Val)
TTN-AS1 NR_038272.1 -?/. - n.2043+7876T>A r.(?) -


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